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Ebba Lohmann

Showing results (11-20 of 77) with videos related to

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Journal of Neurology|May 11, 2015
Clinical variability in ataxia-telangiectasiaEbba Lohmann, Stefanie Krüger, Ann-Kathrin Hauser, et al.
Stem Cell Reports|April 3, 2018
Functional Studies of Missense TREM2 Mutations in Human Stem Cell-Derived MicrogliaPhilip W Brownjohn, James Smith, Ravi Solanki, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 24, 2014
Unusual variability of PRRT2 linked phenotypes within a familyFrieder Brueckner, Bernhard Kohl, Burkhard Puest, et al.
Neurobiology of Aging|July 23, 2013
Novel compound heterozygous mutation in TREM2 found in a Turkish frontotemporal dementia-like familyRita Guerreiro, Basar Bilgic, Gamze Guven, et al.
Human Mutation|October 28, 2006
Deletion of the parkin and PACRG gene promoter in early-onset parkinsonismSuzanne Lesage, Periquet Magali, Ebba Lohmann, et al.
Brain : a Journal of Neurology|January 13, 2006
Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North AfricaPablo Ibáñez, Suzanne Lesage, Ebba Lohmann, et al.
Molecular Biology Reports|July 19, 2020
Peripheral TREM2 mRNA levels in early and late-onset Alzheimer disease's patientsGamze Guven, Basar Bilgic, Bedia Samanci, et al.
American Journal of Alzheimer'S Disease and Other Dementias|July 2, 2013
Reduced orexin-A levels in frontotemporal dementia: possible association with sleep disturbanceArzu Çoban, Basar Bilgiç, Ebba Lohmann, et al.
Journal of Medical Genetics|March 8, 2024
Dissecting genetic architecture of rare dystonia: genetic, molecular and clinical insightsBurcu Atasu, Javier Simón-Sánchez, Hasmet Hanagasi, et al.
Noro Psikiyatri Arsivi|April 1, 2017
The Relationship of White Matter Hyperintensities with Depressive Symptoms and Daily Living Activities in Early-Stage Alzheimer's Disease PatientsBaşar Bilgiç, Ali Bayram, Haşmet A Hanağasi, et al.
Pageof 8

Showing results (11-20 of 77) with videos related to

Sort By:
Pageof 8
Journal of Neurology|May 11, 2015
Clinical variability in ataxia-telangiectasiaEbba Lohmann, Stefanie Krüger, Ann-Kathrin Hauser, et al.
Stem Cell Reports|April 3, 2018
Functional Studies of Missense TREM2 Mutations in Human Stem Cell-Derived MicrogliaPhilip W Brownjohn, James Smith, Ravi Solanki, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 24, 2014
Unusual variability of PRRT2 linked phenotypes within a familyFrieder Brueckner, Bernhard Kohl, Burkhard Puest, et al.
Neurobiology of Aging|July 23, 2013
Novel compound heterozygous mutation in TREM2 found in a Turkish frontotemporal dementia-like familyRita Guerreiro, Basar Bilgic, Gamze Guven, et al.
Human Mutation|October 28, 2006
Deletion of the parkin and PACRG gene promoter in early-onset parkinsonismSuzanne Lesage, Periquet Magali, Ebba Lohmann, et al.
Brain : a Journal of Neurology|January 13, 2006
Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North AfricaPablo Ibáñez, Suzanne Lesage, Ebba Lohmann, et al.
Molecular Biology Reports|July 19, 2020
Peripheral TREM2 mRNA levels in early and late-onset Alzheimer disease's patientsGamze Guven, Basar Bilgic, Bedia Samanci, et al.
American Journal of Alzheimer'S Disease and Other Dementias|July 2, 2013
Reduced orexin-A levels in frontotemporal dementia: possible association with sleep disturbanceArzu Çoban, Basar Bilgiç, Ebba Lohmann, et al.
Journal of Medical Genetics|March 8, 2024
Dissecting genetic architecture of rare dystonia: genetic, molecular and clinical insightsBurcu Atasu, Javier Simón-Sánchez, Hasmet Hanagasi, et al.
Noro Psikiyatri Arsivi|April 1, 2017
The Relationship of White Matter Hyperintensities with Depressive Symptoms and Daily Living Activities in Early-Stage Alzheimer's Disease PatientsBaşar Bilgiç, Ali Bayram, Haşmet A Hanağasi, et al.
Pageof 8